KEGG pathway | spot no | Ac. No. | Name | ratio | P value | Related Neurological disease |
---|---|---|---|---|---|---|
Glycolysis/Gluconeogenesis pathway | 387 | P09972 | Fructose-bisphosphate aldolase C [Homo sapiens] | 1.69 | 0.0009 | Schizophrenia, bipolar disorder, and depression [100] |
 | 471 | P00338 | L-lactate dehydrogenase A chain [Homo sapiens] | 1.5 | 0.039 |  |
 | 439 | P07195 | L-lactate dehydrogenase B chain (LDH) [Homo sapiens] | 1.43 | 0.028 |  |
 | 412 | P14550 | Alcohol dehydrogenase [NADP+] [Homo sapiens] | 1.36 | 0.028 |  |
 | 605 | P60174 | Triosephosphate isomerase [Homo sapiens] | -1.32 | 0.02 | Neurodegeneration [101] |
 | 581 | Q53G35 | Phosphoglycerate mutase 1 (Brain) variant (Fragment) [Homo sapiens] | -1.6 | 0.043 | AD [102] |
Oxidative phosphorylation pathway | 518 | B3KP20 | cDNA FLJ30970 fis, clone HEART2000444, highly similar to Homo sapiens phospholysine phosphohistidine inorganic pyrophosphate phosphatase (LHPP), mRNA [Homo sapiens] | 1.57 | 0.043 | AD [85] |
 | 522 | P36543 | V-type proton ATPase subunit E 1 [Homo sapiens] | 1.55 | 0.0068 |  |
 | 658 | O75947-2 | (ATP5H)Isoform 2 of O75947. [Homo sapiens] | 1.48 | 0.015 |  |
 | 587 | P47985 | Cytochrome b-c1 complex subunit Rieske, mitochondrial [Homo sapiens] | 1.38 | 0.013 |  |
 | 634 | O96000 | NADH dehydrogenase (ubiquinone) 1 beta subcomplex subunit 10 [Homo sapiens] | -1.42 | 0.0059 |  |
Nitrogen metabolism pathway | 363 | P15104 | Glutamine synthetase [Homo sapiens] | 1.85 | 0.0007 | AD [20] |
 | 578 | P00918 | Carbonic anhydrase 2 [Homo sapiens] | -3.11 | 0.009 | Mental retardation, |
Arachidonic acid metabolism pathway | 494 | P16152 | Carbonyl r Carbonyl reductase [NADPH] 1 [Homo sapiens] | 2 | 0.014 | AD [105] |
Purine metabolism pathway | 787 | P22392 | Nucleoside diphosphate kinase B [Homo sapiens] | -1.33 | 0.0061 | DS, AD [106] |
Arginine and proline metabolism pathway | 369 | P12532 | Creatine kinase, ubiquitous mitochondrial [Homo sapiens] | 1.47 | 0.0006 | Alzheimer's and Pick's Disease [17] |
Glutathione metabolism pathway | 624 | P09211 | Glutathione S-transferase P [Homo sapiens] | -1.64 | 0.024 | |
MAPK signalling pathway | 738 | P16949 | Stathmin [Homo sapiens] | 1.48 | 0.031 | |
 | 608 | P62993 | Growth factor receptor-bound protein 2 [Homo sapiens] | 1.29 | 0.04 | AD [110] |
Calcium signalling pathway | 496 | B4DKM5 | cDNA FLJ60120, highly similar to Voltage-dependent anion-selective channel protein 2 [Homo sapiens]* | 1.57 | 0.021 | Â |
 | 411 | P50148 | Guanine nucleotide-binding Protein G(o) subunit alpha [Homo sapiens] | 1.36 | 0.026 | Familial Alzheimer's disease [49] |
Axon guidance pathway | 230 | Q16555 | Dihydropyrimidinase-related protein 2 [Homo sapiens] | 1.57 | 0.025 | AD [14] |
Parkinson's disease pathway | 384 | Q7KYV2 | H5 [Homo sapiens]* | 1.37 | 0.035 | Autosomal-recessive juvenile parkinsonism [111] |
Antigen processing and presentation pathway | 189 | P11142 | Heat shock cognate 71 kDa protein [Homo sapiens] | 1.39 | 0.022 | AD [59] |
N/A | 393 | O00154 | (ACOT7)Isoform 6 of O00154. [Homo sapiens] | 1.64 | 0.0018 | Â |
 | 394 | Q2TU84 | Aspartate aminotransferase [Homo sapiens] | 1.51 | 0.0048 |  |
 | 350 | P49411 | Elongation factor Tu, mitochondrial [Homo sapiens] | 1.35 | 0.008 | Infantile Encephalopathy [24] |
 | 723 | P61601 | Neurocalcin-delta [Homo sapiens]* | 1.57 | 0.043 | AD [53] |
 | 475 | B4DGP9 | cDNA FLJ54102, highly similar to Beta-soluble NSF attachment protein [Homo sapiens] | 1.53 | 0.033 |  |
 | 458 | P62879 | Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-2 [Homo sapiens] | 1.73 | 0.0089 | AD [46] |
 | 784 | A8MVL5 | Putative uncharacterized protein PRDX5 [Homo sapiens] | -1.88 | 0.032 |